Alzheimer's Disease Center Research Registry

Updated on 23 September 2022
Emma Pollner
Primary Contact
Online Study Center (online study) Contact
mild dementia
Online studies
Accepts healthy volunteers


This study is looking for people over the age of 55 who have normal cognition, memory problems, or mild dementia. The study is also looking for people who are care partners of someone who has dementia. The study is intended to match people with studies that may be a good fit for them. 


Study schedule:
-You will visit the study website and enter some demographic, health, and cognitive information.
-If and when a research study that may be a good fit for you becomes available, you will be notified with information about how to sign up.

Study activities may include:
-Using the internet.
-Completing questionnaires about your demographics, health, thinking, and language.

Treatment or experiment details:
-There is no experiment or treatment being tested in this study.
-Study opportunities that you may be offered in the future may require a single visit, or may require more frequent visits (several times a year or annually).
-You are under no obligation to participate in any of the research studies that you receive invitations for in the future. 

Condition Memory Concerns, Memory Problems, Healthy Volunteers, Mild Dementia, Mild Cognitive Impairment, Dementia
Clinical Study IdentifierTX284496
Last Modified on23 September 2022


Yes No Not Sure

Inclusion Criteria

Age 55 or older
You have a ‘study partner’—a friend or family member who would be willing to answer questions about you
You either: have mild memory problems or mild dementia, are healthy and have no memory problems or dementia, are the care partner of someone with dementia

Exclusion Criteria

You have had a serious neurological or medical condition, such as meningitis, encephalitis, neurosyphilis, or a brain tumor
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How to participate?

Step 1 Connect with a study center
What happens next?
  • You can expect the study team to contact you via email or phone in the next few days.
  • Sign up as volunteer  to help accelerate the development of new treatments and to get notified about similar trials.

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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

Learn more

If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

Learn more

Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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